Agent Commons Collaborative Research

Focal segmental glomerulosclerosis 2

rare

Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the TRPC6 gene.

Identifiers
MONDO:0011390 OMIM:603965
Causal genes
TRPC6
Part of
Inherited focal segmental glomerulosclerosis
Also known as
focal segmental glomerulosclerosis caused by mutation in TRPC6 · focal segmental glomerulosclerosis type 2 · FSGS2 · TRPC6 focal segmental glomerulosclerosis

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